Deletion analysis of the simple tandem repeat loci physically linked to the spinal muscular atrophy locus

被引:0
|
作者
Capon, F
Levato, C
Bussaglia, E
LoCicero, S
Tizzano, EF
Baiget, M
Silani, V
Pizzuti, A
Novelli, G
Dallapiccola, B
机构
[1] UNIV ROMA TOR VERGATA, DIPARTIMENTO SANITA PUBBL & BIOL CELLULARE, I-00161 ROME, ITALY
[2] UNIV MILAN, IRCCS SAN GIOVANNI ROTONDO, OSPEDALE CSS, IST NEUROL, MILAN, ITALY
[3] HOSP SANTA CRUZ & SAN PABLO, UNITAT GENT MOLEC, E-08025 BARCELONA, SPAIN
[4] UNIV CATTOLICA SACRO CUORE, CATTEDRA GENET UMANA, I-00168 ROME, ITALY
关键词
spinal muscular atrophy; SMA; simple tandem repeats; STRs; gene deletions;
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Multicopy dinucleotide repeats have been characterized in the spinal muscular atrophy (SMA) region on chromosome 5q13, which reveal deletions in some SMA patients. 119 Italian and Spanish SMA families have been analysed using the C272 and C212 markers, Seventy percent of these families were informative. We found 9.4% de novo deletions in SMA I and 1.5% in SMA II families. A single inherited deletion segregating in a Spanish pedigree was detected in three affected brothers. A SMA II patient showed deletion only of C272. The data presented in this study are relevant to the molecular diagnosis of SMA familes in Italy and Spain and provide additional insights toward the understanding of the molecular pathology of SMA. (C) 1996 Wiley-Liss, Inc.
引用
收藏
页码:198 / 201
页数:4
相关论文
共 50 条
  • [1] 2 5Q13 SIMPLE TANDEM REPEAT LOCI ARE IN LINKAGE DISEQUILIBRIUM WITH TYPE-1 SPINAL MUSCULAR-ATROPHY
    MCLEAN, MD
    ROY, N
    MACKENZIE, AE
    SALIH, M
    BURGHES, AHM
    SIMARD, L
    KORNELUK, RG
    IKEDA, JE
    SURH, L
    [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (11) : 1951 - 1956
  • [2] Identification of an X-linked distal spinal muscular atrophy locus
    Garbern, James
    Shy, Michael
    Krajewski, Karen
    El-Khechen, Dima
    Ebrahim, Salah
    Nicholson, Garth
    Kennerson, Marina
    [J]. NEUROLOGY, 2008, 70 (11) : A137 - A138
  • [3] Deletion analysis in Turkish patients with spinal muscular atrophy
    Erdem, H
    Pehlivan, S
    Topaloglu, H
    Özgüç, M
    [J]. BRAIN & DEVELOPMENT, 1999, 21 (02): : 86 - 89
  • [4] Deletion analysis of spinal muscular atrophy in southern Indian population
    Swaminathan, Bhairavi
    Shylashree, S.
    Purushottam, Meera
    Taly, A. B.
    Nalini, A.
    [J]. NEUROLOGY INDIA, 2008, 56 (03) : 348 - 351
  • [5] Deletion analysis in Iranian patients with spinal muscular atrophy type I
    Barzegar, Mohammad
    Bonyadi, Mortaza Jabbarpour
    Jameii, Ahmad
    [J]. NEUROMUSCULAR DISORDERS, 2006, 16 : S116 - S116
  • [6] ANALYSIS OF YACS FROM THE VICINITY OF THE SPINAL MUSCULAR-ATROPHY LOCUS
    BOYCE, FM
    LIEN, L
    MONACO, A
    KLEYN, P
    BRZUSTOWICZ, LM
    GILLIAM, TC
    KUNKEL, LM
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 375 - 375
  • [7] Genetic analysis of three short tandem repeat loci and one variable number of tandem repeat locus in the Korean population
    Kim, KS
    Kim, MH
    Choi, SM
    Chi, SE
    Cho, DW
    [J]. KOREAN JOURNAL OF GENETICS, 1999, 21 (01): : 41 - 48
  • [8] DELETION ANALYSIS OF THE SMN GENE IN INFANTILE AND ADULT SPINAL MUSCULAR-ATROPHY
    BRAHE, C
    ZAPPATA, S
    TIZIANO, F
    GANDOLFI, N
    PARAVATOUPETSOTAS, M
    NERI, G
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 1199 - 1199
  • [9] Deletion analysis of SMN and NAIP genes in Tunisian patients with spinal muscular atrophy
    Rekik, Imen
    Boukhris, Amir
    Ketata, Sourour
    Amri, Mohamed
    Essid, Nourhene
    Feki, Imed
    Mhiri, Chokri
    [J]. ANNALS OF INDIAN ACADEMY OF NEUROLOGY, 2013, 16 (01) : 57 - 61
  • [10] Deletion analysis of the SMN and NAIP genes in Kuwaiti patients with spinal muscular atrophy
    Samilchuk, E
    DSouza, B
    Bastaki, L
    AlAwadi, S
    [J]. HUMAN GENETICS, 1996, 98 (05) : 524 - 527